Publications
Found 7 results
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“Copy number variations in spermatogenic failure patients with chromosomal abnormalities and unexplained azoospermia”, vol. 14, pp. 16041-16049, 2015.
, “Reproductive outcome of a case with familial balanced translocation t(3;6): implications for genetic counseling”, vol. 14, pp. 2809-2815, 2015.
, “Result and pedigree analysis of spontaneously abortion villus chromosome detecting by FISH”, vol. 14, pp. 16662-16666, 2015.
, “Sperm aneuploidy and implications for genetic counseling in a pedigree of three t(1;3) balanced translocation carriers”, vol. 14, pp. 5003-5009, 2015.
, “Sperm retrieval from patients with nonmosaic Klinefelter’s syndrome by semen cytology examination”, vol. 13, pp. 1848-1854, 2014.
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“Correlation of Y-chromosome multiple segmental deletions and chromosomal anomalies in non-obstructive azoospermic males from northeastern China”, vol. 11, pp. 2422-2431, 2012.
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Balaresque P, Bowden GR, Parkin EJ, Omran GA, et al. (2008). Dynamic nature of the proximal AZFc region of the human Y chromosome: multiple independent deletion and duplication events revealed by microsatellite analysis. Hum. Mutat. 29: 1171-1180.
http://dx.doi.org/10.1002/humu.20757
PMid:18470947 PMCid:2689608
Balkan M, Tekes S and Gedik A (2008). Cytogenetic and Y chromosome microdeletion screening studies in infertile males with Oligozoospermia and Azoospermia in Southeast Turkey. J. Assist. Reprod. Genet. 25: 559-565.
http://dx.doi.org/10.1007/s10815-008-9272-8
PMid:18953646 PMCid:2593766
Briton-Jones C and Haines CJ (2000). Microdeletions on the long arm of the Y chromosome and their association with male-factor infertility. Hong Kong Med. J. 6: 184-189.
PMid:10895142
Chiang HS, Yeh SD, Wu CC, Huang BC, et al. (2004). Clinical and pathological correlation of the microdeletion of Y chromosome for the 30 patients with azoospermia and severe oligoasthenospermia. Asian J. Androl. 6: 369-375.
PMid:15546032
Devroey P, Fauser BC and Diedrich K (2009). Approaches to improve the diagnosis and management of infertility. Hum. Reprod. Update 15: 391-408.
http://dx.doi.org/10.1093/humupd/dmp012
PMid:19380415 PMCid:2691653
Ferlin A, Arredi B, Speltra E, Cazzadore C, et al. (2007). Molecular and clinical characterization of Y chromosome microdeletions in infertile men: a 10-year experience in Italy. J. Clin. Endocrinol. Metab. 92: 762-770.
http://dx.doi.org/10.1210/jc.2006-1981
PMid:17213277
Foresta C, Ferlin A and Moro E (2000). Deletion and expression analysis of AZFa genes on the human Y chromosome revealed a major role for DBY in male infertility. Hum. Mol. Genet. 9: 1161-1169.
http://dx.doi.org/10.1093/hmg/9.8.1161
PMid:10767340
Foresta C, Moro E and Ferlin A (2001). Y chromosome microdeletions and alterations of spermatogenesis. Endocr. Rev. 22: 226-239.
http://dx.doi.org/10.1210/er.22.2.226
PMid:11294825
Gatta V, Stuppia L, Calabrese G, Morizio E, et al. (2002). A new case of Yq microdeletion transmitted from a normal father to two infertile sons. J. Med. Genet. 39: E27.
http://dx.doi.org/10.1136/jmg.39.6.e27
PMid:12070259 PMCid:1735151
Imken L, El HB, Chafik A, Nahili H, et al. (2007). AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men. Asian J. Androl. 9: 674-678.
http://dx.doi.org/10.1111/j.1745-7262.2007.00290.x
PMid:17712485
Kato H, Komori S, Nakata Y, Sakata K, et al. (2001). Screening for deletions in interval D16-22 of the Y chromosome in azoospermic and oligozoospermic Japanese men. J. Hum. Genet. 46: 110-114.
http://dx.doi.org/10.1007/s100380170097
PMid:11310577
Kent-First M, Muallem A, Shultz J, Pryor J, et al. (1999). Defining regions of the Y-chromosome responsible for male infertility and identification of a fourth AZF region (AZFd) by Y-chromosome microdeletion detection. Mol. Reprod. Dev. 53: 27-41.
http://dx.doi.org/10.1002/(SICI)1098-2795(199905)53:1<27::AID-MRD4>3.0.CO;2-W
Kihaile PE, Yasui A and Shuto Y (2005). Prospective assessment of Y-chromosome microdeletions and reproductive outcomes among infertile couples of Japanese and African origin. J. Exp. Clin. Assist. Reprod. 2: 9.
http://dx.doi.org/10.1186/1743-1050-2-9
PMid:15987528 PMCid:1198247
Krausz C, Rajpert-De ME, Frydelund-Larsen L, Quintana-Murci L, et al. (2001). Double-blind Y chromosome microdeletion analysis in men with known sperm parameters and reproductive hormone profiles: microdeletions are specific for spermatogenic failure. J. Clin. Endocrinol. Metab. 86: 2638-2642.
http://dx.doi.org/10.1210/jc.86.6.2638
PMid:11397865
Krausz C, Forti G and McElreavey K (2003). The Y chromosome and male fertility and infertility. Int. J. Androl. 26: 70-75.
http://dx.doi.org/10.1046/j.1365-2605.2003.00402.x
PMid:12641824
Le Bourhis C, Siffroi JP, McElreavey K and Dadoune JP (2000). Y chromosome microdeletions and germinal mosaicism in infertile males. Mol. Hum. Reprod. 6: 688-693.
http://dx.doi.org/10.1093/molehr/6.8.688
PMid:10908277
Lin YM, Chen CW, Sun HS, Hsu CC, et al. (2000). Y-chromosome microdeletion and its effect on reproductive decisions in taiwanese patients presenting with nonobstructive azoospermia. Urology 56: 1041-1046.
http://dx.doi.org/10.1016/S0090-4295(00)00846-3
Lin YM, Lin YH, Teng YN, Hsu CC, et al. (2002). Gene-based screening for Y chromosome deletions in Taiwanese men presenting with spermatogenic failure. Fertil. Steril. 77: 897-903.
http://dx.doi.org/10.1016/S0015-0282(02)03059-5
Mafra FA, Christofolini DM, Bianco B, Gava MM, et al. (2011). Chromosomal and molecular abnormalities in a group of Brazilian infertile men with severe oligozoospermia or non-obstructive azoospermia attending an infertility service. Int. Braz. J. Urol. 37: 244-250.
http://dx.doi.org/10.1590/S1677-55382011000200011
PMid:21557841
Martinez MC, Bernabe MJ, Gomez E, Ballesteros A, et al. (2000). Screening for AZF deletion in a large series of severely impaired spermatogenesis patients. J. Androl. 21: 651-655.
PMid:10975411
Medica I, Gligorievska N, Prenc M and Peterlin B (2005). Y microdeletions in the Istria county, Croatia. Asian J. Androl. 7: 213-216.
http://dx.doi.org/10.1111/j.1745-7262.2005.00028.x
PMid:15897979
Mirfakhraie R, Mirzajani F, Kalantar SM, Montazeri M, et al. (2010). High prevalence of AZFb microdeletion in Iranian Y-chromosome microdeletions and chromosomal anomalies patients with idiopathic non-obstructive azoospermia. Ind. J. Med. Res. 132: 265-270.
PMid:20847372
Mitra A, Dada R, Kumar R, Gupta NP, et al. (2008). Screening for Y-chromosome microdeletions in infertile Indian males: utility of simplified multiplex PCR. Ind. J. Med. Res. 127: 124-132.
PMid:18403789
Organization WH (1999). Laboratory Manual for the Examination of Human Semen and Semen-Cervical Mucus Interaction. Cambridge University Press, Cambridge.
Osterlund C, Segersteen E, Arver S and Pousette A (2000). Low number of Y-chromosome deletions in infertile azoospermic men at a Swedish andrology centre. Int. J. Androl. 23: 225-229.
http://dx.doi.org/10.1046/j.1365-2605.2000.00234.x
PMid:10886425
Peterlin B, Kunej T and Hristovski D (2004). Diagnostic test for Y chromosome microdeletion screening in male infertility. Genet. Test. 8: 45-49.
http://dx.doi.org/10.1089/109065704323016021
PMid:15140373
Shaffer LG, Slovak ML and Campbell LJ (2009). ISCN 2009: An International System for Human Cytogenetic Nomenclature, Karger.
Simoni M, Bakker E and Krausz C (2004). EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004. Int. J. Androl. 27: 240-249.
http://dx.doi.org/10.1111/j.1365-2605.2004.00495.x
PMid:15271204
Tiepolo L and Zuffardi O (1976). Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm. Hum. Genet. 34: 119-124.
http://dx.doi.org/10.1007/BF00278879
PMid:1002136
Tsujimura A, Matsumiya K, Takao T, Miyagawa Y, et al. (2004). Clinical analysis of patients with azoospermia factor deletions by microdissection testicular sperm extraction. Int. J. Androl. 27: 76-81.
http://dx.doi.org/10.1046/j.0105-6263.2003.00450.x
PMid:15149464
Vicdan A, Vicdan K, Gunalp S, Kence A, et al. (2004). Genetic aspects of human male infertility: the frequency of chromosomal abnormalities and Y chromosome microdeletions in severe male factor infertility. Eur. J. Obstet. Gynecol. Reprod. Biol. 117: 49-54.
http://dx.doi.org/10.1016/j.ejogrb.2003.07.006
PMid:15474244
Vutyavanich T, Piromlertamorn W, Sirirungsi W and Sirisukkasem S (2007). Frequency of Y chromosome microdeletions and chromosomal abnormalities in infertile Thai men with oligozoospermia and azoospermia. Asian J. Androl. 9: 68-75.
http://dx.doi.org/10.1111/j.1745-7262.2007.00239.x
PMid:17187159
Yang Y, Ma MY, Xiao CY, Li L, et al. (2008). Massive deletion in AZFb/b+c and azoospermia with Sertoli cell only and/ or maturation arrest. Int. J. Androl. 31: 573-578.
http://dx.doi.org/10.1111/j.1365-2605.2007.00808.x
PMid:17877719